formulate trial accounting balances | make trial accounting balances ready | calculate trial accounting balances | prepare trial accounting balances

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

préparer des balances de comptes

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

The Brand and Brand Inspection Act [ An Act respecting Brands and Brand Inspection ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

The Brand and Brand Inspection Act [ An Act respecting Brands and Brand Inspection ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

brand strategy [ branding | brand building | brand development ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

stratégie de marque [ valorisation de la marque | branding ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

IN-CONTEXT TRANSLATIONS

Ninth, require that all companies, both branded and unbranded, that manufacturer or distribute opioids, sedatives, hypnotics or stimulants comply with full drug submission requirements before listings, and that would include the provision for branded and unbranded clinical trials, and give that data to Health Canada.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-05]

Neuvièmement, avant l'inscription de produits sur les listes, obliger toutes les entreprises qui fabriquent ou distribuent des opioïdes, des sédatifs, des hypnotiques ou des stimulants, qu'il s'agisse de produits de marque ou génériques, à se conformer à toutes les exigences relatives à la présentation de drogues — ce qui comprend la réalisation d'essais cliniques — et à fournir les données pertinentes à Santé Canada.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-05]

http://www.parl.gc.ca/Content/ (...) [HTML] [2014-09-05]

They should also require that generic manufacturers complete clinical trials to ensure the safety of their product is comparable to the brand.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-05]

Il faudrait également obliger les fabricants de produits génériques à effectuer des essais cliniques afin de s'assurer que leur produit est aussi sûr que le médicament de marque.

http://www.parl.gc.ca/content/ (...) (...) [HTML] [2014-09-05]

http://www.parl.gc.ca/Content/ (...) [HTML] [2014-09-05]

On those trials, again, if you involve a veterinary school in measuring it and maybe even the public health surveillance unit, the C-EnterNet that's in place, the other component that people are interested in building in is some of the brand-specific things.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2009-05-26]

Pour poursuivre à propos des essais, il peut être intéressant d'obtenir la participation d'une école vétérinaire et peut-être même de l'unité de surveillance de la santé publique, ce qu'on appelle le C-EnterNet.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2009-05-26]

http://www.parl.gc.ca/HousePub (...) [HTML] [2009-05-26]

This is of vital importance to generic companies because unlike brand-name drugs that are approved on the basis of lengthy and costly clinical trial studies, generic drugs are approved simply on the basis of bioequivalence comparisons to the already approved brand drug.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2003-06-01]

Cette exception est d'une importance capitale pour les fabricants de médicaments génériques parce que, contrairement aux médicaments d'origine qui ne sont approuvés qu'après de longues et de coûteuses études cliniques, les médicaments génériques sont approuvés sur la base des comparaisons de la bio-équivalence par rapport aux médicaments d'origine déjà approuvés.

http://www.parl.gc.ca/HousePub (...) (...) [HTML] [2003-06-01]

http://www.parl.gc.ca/HousePub (...) [HTML] [2003-06-01]

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A bioequivalence trial is the sort of trial you perform to show whether a generic medicine performs the same as a branded medicine.

http://www.parl.gc.ca/content/ (...) (...) [HTML]

Les essais de bioéquivalence, ce sont des essais qui visent à prouver qu'un médicament générique donne les mêmes résultats qu'un médicament de marque.

http://www.parl.gc.ca/content/ (...) (...) [HTML]

http://www.parl.gc.ca/Content/ (...) [HTML]

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Date index: 2023-10-13